Therapeutic angiogenesis using tumor cell-conditioned medium

被引:8
|
作者
Jang, Hyeon-Ki [1 ]
Han, Jin [2 ]
Yoon, Jeong-Kee [2 ]
Lee, Ju-Ro [2 ]
Jeong, Gun-Jae [2 ]
Shin, Jung-Youn [2 ,4 ]
Kim, Byung-Soo [1 ,2 ,3 ]
机构
[1] Seoul Natl Univ, Interdisciplinary Program Bioengn, Seoul 151744, South Korea
[2] Seoul Natl Univ, Sch Chem & Biol Engn, Seoul 151744, South Korea
[3] Seoul Natl Univ, Inst Chem Proc, BioMAX Inst, Seoul 151744, South Korea
[4] Case Western Reserve Univ, Dept Biomed Engn, Cleveland, OH 44106 USA
基金
新加坡国家研究基金会;
关键词
mesenchymal stem cell; ischemia; therapeutic angiogenesis; tumor cell-conditioned medium; MESENCHYMAL STEM-CELLS; ENDOTHELIAL PROGENITOR CELLS; GROWTH-FACTOR; IN-VITRO; PROMOTES ANGIOGENESIS; CANCER; REVASCULARIZATION; LIMITATIONS; ACTIVATION; DELIVERY;
D O I
10.1002/btpr.2226
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Stem cell-conditioned medium (CM), which contains angiogenic factors that are secreted by stem cells, represents a potential therapy for ischemic diseases. Along with stem cells, tumor cells also secrete various angiogenic factors. Here, tumor cells as a cell source of CM for therapeutic angiogenesis was evaluated and the therapeutic efficacy of tumor cell CM in mouse hindlimb ischemia models was demonstrated. CM obtained from a human fibrosarcoma HT1080 cell line culture was compared with CM obtained from a human bone marrow-derived mesenchymal stem cell (MSC) culture. HT1080 CM contained higher concentrations of angiogenic factors compared with MSC CM, which was attributable to the higher cell density that resulted from a much faster growth rate of HT1080 cells compared with MSCs. For use in in vitro and in vivo angiogenesis studies, HT1080 CM was diluted such that HT1080 CM and MSC CM would have the same cell number basis. The two types of CMs induced the same extent of human umbilical vein endothelial cell (HUVEC) proliferation in vitro. The injection of HT1080 CM into mouse ischemic limbs significantly improved capillary density and blood perfusion compared with the injection of fresh medium. Although the therapeutic outcome of HT1080 CM was similar to that of MSC CM, the preparation of CM by tumor cell line culture would be much more efficient due to the faster growth and unlimited life-time of the tumor cell line. These data suggest the potential application of tumor cell CM as a therapeutic modality for angiogenesis and ischemic diseases. (c) 2016 American Institute of Chemical Engineers Biotechnol. Prog., 32:456-464, 2016
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页码:456 / 464
页数:9
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